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SARS-CoV-2 nasopharyngeal viral load in individuals infected with BA.2, compared to Alpha, Gamma, Delta and BA.1 variants: A single-center comparative analysis.
Mastrorosa, Ilaria; Cozzi-Lepri, Alessandro; Colavita, Francesca; Lalle, Eleonora; Mazzotta, Valentina; Cimaglia, Claudia; Paulicelli, Jessica; Matusali, Giulia; Fabeni, Lavinia; Carletti, Fabrizio; Rosati, Silvia; Vita, Serena; Giannico, Giuseppina; Piselli, Pierluca; Biliotti, Elisa; Moghazi, Samir Al; Mosti, Silvia; Girardi, Enrico; Nicastri, Emanuele; Garbuglia, Anna Rosa; Maggi, Fabrizio; Vaia, Francesco; Antinori, Andrea.
  • Mastrorosa I; Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy. Electronic address: ilaria.mastrorosa@inmi.it.
  • Cozzi-Lepri A; Centre for Clinical Research, Epidemiology, Modelling and Evaluation (CREME), Institute for Global Health, UCL, London, United Kingdom.
  • Colavita F; Laboratory of Virology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Lalle E; Laboratory of Virology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Mazzotta V; Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Cimaglia C; Department of Epidemiology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Paulicelli J; Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Matusali G; Laboratory of Virology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Fabeni L; Laboratory of Virology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Carletti F; Laboratory of Virology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Rosati S; Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Vita S; Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Giannico G; Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Piselli P; Department of Epidemiology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Biliotti E; Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Moghazi SA; Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Mosti S; Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Girardi E; Department of Epidemiology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy; Scientific Direction, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Nicastri E; Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Garbuglia AR; Laboratory of Virology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Maggi F; Laboratory of Virology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Vaia F; General Direction, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
  • Antinori A; Clinical and Research Infectious Diseases Department, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Via Portuense 292, Rome 00149, Italy.
J Clin Virol ; 157: 105299, 2022 Dec.
Article in English | MEDLINE | ID: covidwho-2041915
ABSTRACT

BACKGROUND:

SARS-CoV-2 has evolved, leading to the emergence of new Variants Of Concern (VOCs) with significant impact on transmissibility. Although the transmission process is complex, higher nasopharyngeal viral load (NP-VL) can be considered as a proxy for greater transmissibility.

OBJECTIVES:

The aim of this analysis was to compare NP-VL across a set of representative VOCs observed in mildly symptomatic patients. STUDY

DESIGN:

Observational single-center comparative analysis of patients with early mild-to-moderate COVID-19, enrolled within the early treatment access program of Lazzaro Spallanzani Institute (March 2021-March 2022). NP-VL before drug administration was estimated through RT-PCR, based on cycle threshold values (CTs); VOCs were identified by Sanger sequencing. VOCs' average treatment effect (ATE) was estimated on the CTs fitted in the log2 scale, controlling for potential confounders.

RESULTS:

A total of 707 patients were included. VOCs were 10% Alpha, 3% Gamma, 34% Delta, 34% BA.1, 19% BA.2. Mean CTs for BA.1 and BA.2 were lower than Delta and BA.1, respectively. After adjusting for calendar time, age, immunodeficiency and vaccination, CTs for Gamma were lower than those seen for Alpha and higher than Delta, for Delta were similar to BA.1, for BA.2 were lower than Delta and BA.1.

CONCLUSIONS:

Our analysis shows higher NP-VL of BA.2 compared to previously circulating VOCs, even after controlling for factors potentially contributing to the amount of nasopharyngeal viral RNA, included vaccination, supporting the increased transmissibility of BA.2. Further studies are necessary to clarify this mechanism and to provide guidance for public health measures.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: J Clin Virol Journal subject: Virology Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: J Clin Virol Journal subject: Virology Year: 2022 Document Type: Article